Product NDC: | 59365-5030 |
Proprietary Name: | TRIMO SAN |
Non Proprietary Name: | Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
Active Ingredient(s): | .25; .01 g/g; g/g & nbsp; Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | JELLY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59365-5030 |
Labeler Name: | CooperSurgical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19770401 |
Package NDC: | 59365-5030-0 |
Package Description: | 113.4 g in 1 TUBE (59365-5030-0) |
NDC Code | 59365-5030-0 |
Proprietary Name | TRIMO SAN |
Package Description | 113.4 g in 1 TUBE (59365-5030-0) |
Product NDC | 59365-5030 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
Dosage Form Name | JELLY |
Route Name | VAGINAL |
Start Marketing Date | 19770401 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | CooperSurgical, Inc. |
Substance Name | OXYQUINOLINE SULFATE; SODIUM LAURYL SULFATE |
Strength Number | .25; .01 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |